-
1
-
-
0036849077
-
The biochemistry and medical significance of the flavonoids
-
Havsteen, B. H. The biochemistry and medical significance of the flavonoids. Pharmacol. Ther. 2002, 96, 67-202.
-
(2002)
Pharmacol. Ther
, vol.96
, pp. 67-202
-
-
Havsteen, B.H.1
-
2
-
-
0033637140
-
The effects of plant flavonoids on mammalian cells: Implications for inflammation, heart disease, and cancer
-
Middleton, E., Jr.; Kandaswami, C.; Theoharides, T. C. The effects of plant flavonoids on mammalian cells: implications for inflammation, heart disease, and cancer. Pharmacol. Rev. 2000, 52, 673-751.
-
(2000)
Pharmacol. Rev
, vol.52
, pp. 673-751
-
-
Middleton Jr., E.1
Kandaswami, C.2
Theoharides, T.C.3
-
3
-
-
27144442384
-
New cytotoxic flavonoids from Thelypteris torresiana
-
Lin, A.-S.; Chang, F.-R.; Wu, C.-C.; Liaw, C.-C.; Wu, Y.-C. New cytotoxic flavonoids from Thelypteris torresiana. Planta Med. 2005, 71, 867-870.
-
(2005)
Planta Med
, vol.71
, pp. 867-870
-
-
Lin, A.-S.1
Chang, F.-R.2
Wu, C.-C.3
Liaw, C.-C.4
Wu, Y.-C.5
-
4
-
-
34548107656
-
-
50 values of protoapigenone toward human breast normal (MCF-10A) and cancer (MCF-7 and MDA-MB-231) cell lines were 8.2 ± 1.0, 1.8 ± 0.1, and 1.1 ± 0.4 μM, respectively.
-
50 values of protoapigenone toward human breast normal (MCF-10A) and cancer (MCF-7 and MDA-MB-231) cell lines were 8.2 ± 1.0, 1.8 ± 0.1, and 1.1 ± 0.4 μM, respectively.
-
-
-
-
5
-
-
0037048763
-
Antiproliferative activities of citrus flavonoids against six human cancer cell lines
-
Manthey, J. A.; Guthrie, N. Antiproliferative activities of citrus flavonoids against six human cancer cell lines. J. Agric Food Chem. 2002, 50, 5837-5843.
-
(2002)
J. Agric Food Chem
, vol.50
, pp. 5837-5843
-
-
Manthey, J.A.1
Guthrie, N.2
-
6
-
-
0037434507
-
4-Substituted 4-hydroxycyclohexa-2, 5-dien-1-one with selective activities against colon and renal cancer cell lines
-
Wells, G.; Berry, J. M.; Bradshaw, T. D.; Burger, A. M.; Seaton, A.; Wang, B.; Westwell, A. D.; Stevens, M. F. G. 4-Substituted 4-hydroxycyclohexa-2, 5-dien-1-one with selective activities against colon and renal cancer cell lines. J. Med. Chem. 2003, 46, 532-541.
-
(2003)
J. Med. Chem
, vol.46
, pp. 532-541
-
-
Wells, G.1
Berry, J.M.2
Bradshaw, T.D.3
Burger, A.M.4
Seaton, A.5
Wang, B.6
Westwell, A.D.7
Stevens, M.F.G.8
-
7
-
-
27844567119
-
Novel reaction products from the hypervalent iodine oxidation of hydroxy stilbenes and isoflavones
-
Lion, C. J.; Vasselin, D. A.; Schwalbe, C. H.; Matthews, C. S.; Stevens, M. F. G.; Westwell, A. D. Novel reaction products from the hypervalent iodine oxidation of hydroxy stilbenes and isoflavones. Org. Biomol. Chem. 2005, 3, 3996-4001.
-
(2005)
Org. Biomol. Chem
, vol.3
, pp. 3996-4001
-
-
Lion, C.J.1
Vasselin, D.A.2
Schwalbe, C.H.3
Matthews, C.S.4
Stevens, M.F.G.5
Westwell, A.D.6
-
8
-
-
12344254823
-
Quinols as novel therapeutic agents. 2. 4-(1-Arylsulfonylindol-2-yl)-4-hydroxycyclohexa-2,5- diene-1-ones and related agents as potent and selective antitumor agents
-
Berry, J. M.; Bradshaw, T. D.; Fichtner, I.; Ren, R.; Schwalbe, C. H.; Wells, G.; Chew, E.-H.; Stevens, M. F. G.; Westwell, A. D. Quinols as novel therapeutic agents. 2. 4-(1-Arylsulfonylindol-2-yl)-4-hydroxycyclohexa-2,5- diene-1-ones and related agents as potent and selective antitumor agents. J. Med. Chem. 2005, 48, 639-644.
-
(2005)
J. Med. Chem
, vol.48
, pp. 639-644
-
-
Berry, J.M.1
Bradshaw, T.D.2
Fichtner, I.3
Ren, R.4
Schwalbe, C.H.5
Wells, G.6
Chew, E.-H.7
Stevens, M.F.G.8
Westwell, A.D.9
-
9
-
-
20944439854
-
Elucidation of thioredoxin as a molecular target for antitumor quinols
-
Bradshaw, T. D.; Matthews, C. S.; Cookson, J.; Chew, E.-H.; Shah, M.; Bailey, K.; Monks, A.; Harris, E.; Westwell, A. D.; Wells, G.; Laughton, C. A.; Stevens, M. F. G. Elucidation of thioredoxin as a molecular target for antitumor quinols. Cancer Res. 2005, 65, 3911-3919.
-
(2005)
Cancer Res
, vol.65
, pp. 3911-3919
-
-
Bradshaw, T.D.1
Matthews, C.S.2
Cookson, J.3
Chew, E.-H.4
Shah, M.5
Bailey, K.6
Monks, A.7
Harris, E.8
Westwell, A.D.9
Wells, G.10
Laughton, C.A.11
Stevens, M.F.G.12
-
10
-
-
25844500308
-
Synthesis and evaluation of antiplatelet activity of trihydroxychalcone derivatives
-
Zhao, L.-M.; Jin, H.-S.; Sun, L.-P.; Piao, H.-R.; Quan, Z.-S. Synthesis and evaluation of antiplatelet activity of trihydroxychalcone derivatives. Bioorg. Med. Chem. 2005, 15, 5027-5029.
-
(2005)
Bioorg. Med. Chem
, vol.15
, pp. 5027-5029
-
-
Zhao, L.-M.1
Jin, H.-S.2
Sun, L.-P.3
Piao, H.-R.4
Quan, Z.-S.5
-
11
-
-
1242339553
-
Synthesis and inhibitory activity against COX-2 catalyzed prostaglandin production of chrysin derivatives
-
Dao, T. T.; Chi, Y. S.; Kim, J.; Kim, H. P.; Kim, S.; Park, H. Synthesis and inhibitory activity against COX-2 catalyzed prostaglandin production of chrysin derivatives. Bioorg. Med. Chem. 2004, 14, 1165-1167.
-
(2004)
Bioorg. Med. Chem
, vol.14
, pp. 1165-1167
-
-
Dao, T.T.1
Chi, Y.S.2
Kim, J.3
Kim, H.P.4
Kim, S.5
Park, H.6
-
12
-
-
0034680718
-
An effective synthesis of isoorientin: The regioselective synthesis of a 6-C-glucosylflavone
-
Kumazawa, T.; Minatogawa, T.; Matsuba, S.; Sato, S.; Onodera, J. An effective synthesis of isoorientin: the regioselective synthesis of a 6-C-glucosylflavone. Carbohydr. Res. 2000, 329, 507-513.
-
(2000)
Carbohydr. Res
, vol.329
, pp. 507-513
-
-
Kumazawa, T.1
Minatogawa, T.2
Matsuba, S.3
Sato, S.4
Onodera, J.5
-
13
-
-
37049084753
-
A simple and efficient procedure for the preparation of p-quinols by hypervalent iodine oxidation of phenols and phenol tripropylsilyl ethers
-
McKillop, A.; McLaren, L.; Taylor, R. J. K. A simple and efficient procedure for the preparation of p-quinols by hypervalent iodine oxidation of phenols and phenol tripropylsilyl ethers. J. Chem. Soc., Perkin Trans. 1 1994, 2047-2048.
-
(1994)
J. Chem. Soc., Perkin Trans. 1
, pp. 2047-2048
-
-
McKillop, A.1
McLaren, L.2
Taylor, R.J.K.3
-
14
-
-
0000630657
-
π-Facial selectivity in nucleophilic additions to 4,4-disubstituted dienones: Experimental support for electrostatic control
-
Wipf, P.; Kim, Y. π-Facial selectivity in nucleophilic additions to 4,4-disubstituted dienones: experimental support for electrostatic control. J. Am. Chem. Soc. 1994, 116, 11678-11688.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 11678-11688
-
-
Wipf, P.1
Kim, Y.2
-
15
-
-
34548098982
-
Methods of synthesizing flavonoids and chalcones. US patent application series
-
no. 20040242907, May 28
-
Shaw, J.; Lee, A.-R.; Huang, W.-H. Methods of synthesizing flavonoids and chalcones. US patent application series no. 20040242907, May 28, 2004.
-
(2004)
-
-
Shaw, J.1
Lee, A.-R.2
Huang, W.-H.3
-
16
-
-
33846828397
-
Fine tuning of a reported synthetic route for biologically active flavonoid, baicalein
-
Kim, S. K.; Sohn, D. W.; Kim, Y. C.; Kim, S.-A.; Lee, S. K.; Kim, H. S. Fine tuning of a reported synthetic route for biologically active flavonoid, baicalein. Arch. Pharm. Res. 2007, 30, 18-21.
-
(2007)
Arch. Pharm. Res
, vol.30
, pp. 18-21
-
-
Kim, S.K.1
Sohn, D.W.2
Kim, Y.C.3
Kim, S.-A.4
Lee, S.K.5
Kim, H.S.6
-
17
-
-
0027405199
-
Comparison of the neutral red and methylene blue assays to study cell growth in culture
-
Elliott, W. M.; Auersperg, N. Comparison of the neutral red and methylene blue assays to study cell growth in culture. Biotech. Histochem. 1993, 68, 29-35.
-
(1993)
Biotech. Histochem
, vol.68
, pp. 29-35
-
-
Elliott, W.M.1
Auersperg, N.2
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